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2
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本文引用的文献

1
Integration of metabolic and gene regulatory networks modulates the C. elegans dietary response.代谢和基因调控网络的整合调节了秀丽隐杆线虫的饮食反应。
Cell. 2013 Mar 28;153(1):253-66. doi: 10.1016/j.cell.2013.02.050.
2
C. elegans feeding.秀丽隐杆线虫的进食
WormBook. 2012 May 21:1-23. doi: 10.1895/wormbook.1.150.1.
3
mTOR signaling in growth control and disease.mTOR 信号在生长控制和疾病中的作用。
Cell. 2012 Apr 13;149(2):274-93. doi: 10.1016/j.cell.2012.03.017.
4
S6K links cell fate, cell cycle and nutrient response in C. elegans germline stem/progenitor cells.S6K 在秀丽隐杆线虫生殖干细胞/祖细胞中连接细胞命运、细胞周期和营养感应。
Development. 2012 Mar;139(5):859-70. doi: 10.1242/dev.074047. Epub 2012 Jan 25.
5
Yeast one-hybrid assays for gene-centered human gene regulatory network mapping.酵母单杂交检测用于基因中心的人类基因调控网络作图。
Nat Methods. 2011 Oct 30;8(12):1050-2. doi: 10.1038/nmeth.1764.
6
Hormone signaling and phenotypic plasticity in nematode development and evolution.线虫发育和进化中的激素信号和表型可塑性。
Curr Biol. 2011 Sep 27;21(18):R758-66. doi: 10.1016/j.cub.2011.06.034.
7
NHR-23 dependent collagen and hedgehog-related genes required for molting.蜕皮需要 NHR-23 依赖的胶原蛋白和刺猬相关基因。
Biochem Biophys Res Commun. 2011 Oct 7;413(4):515-20. doi: 10.1016/j.bbrc.2011.08.124. Epub 2011 Sep 2.
8
Nuclear Receptors: Small Molecule Sensors that Coordinate Growth, Metabolism and Reproduction.核受体:协调生长、代谢和生殖的小分子传感器。
Subcell Biochem. 2011;52:123-53. doi: 10.1007/978-90-481-9069-0_6.
9
Food sensitizes C. elegans avoidance behaviours through acute dopamine signalling.食物通过急性多巴胺信号来敏化秀丽隐杆线虫的回避行为。
EMBO J. 2011 Mar 16;30(6):1110-22. doi: 10.1038/emboj.2011.22. Epub 2011 Feb 8.
10
Genetic and molecular analysis of nematode-microbe interactions.线虫-微生物相互作用的遗传和分子分析。
Cell Microbiol. 2011 Apr;13(4):497-507. doi: 10.1111/j.1462-5822.2011.01570.x. Epub 2011 Jan 30.

饮食诱导的秀丽隐杆线虫的发育加速与 TOR 和胰岛素无关。

Diet-induced developmental acceleration independent of TOR and insulin in C. elegans.

机构信息

Program in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Cell. 2013 Mar 28;153(1):240-52. doi: 10.1016/j.cell.2013.02.049.

DOI:10.1016/j.cell.2013.02.049
PMID:23540701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3821073/
Abstract

Dietary composition has major effects on physiology. Here, we show that developmental rate, reproduction, and lifespan are altered in C. elegans fed Comamonas DA1877 relative to those fed a standard E. coli OP50 diet. We identify a set of genes that change in expression in response to this diet and use the promoter of one of these (acdh-1) as a dietary sensor. Remarkably, the effects on transcription and development occur even when Comamonas DA1877 is diluted with another diet, suggesting that Comamonas DA1877 generates a signal that is sensed by the nematode. Surprisingly, the developmental effect is independent from TOR and insulin signaling. Rather, Comamonas DA1877 affects cyclic gene expression during molting, likely through the nuclear hormone receptor NHR-23. Altogether, our findings indicate that different bacteria elicit various responses via distinct mechanisms, which has implications for diseases such as obesity and the interactions between the human microbiome and intestinal cells.

摘要

饮食组成对生理有重大影响。在这里,我们发现与喂食标准大肠杆菌 OP50 饮食的线虫相比,喂食 Comamonas DA1877 的线虫的发育速度、繁殖和寿命发生了改变。我们鉴定出一组响应这种饮食而改变表达的基因,并使用其中一个基因(acdh-1)的启动子作为饮食传感器。值得注意的是,即使将 Comamonas DA1877 与另一种饮食混合,对转录和发育的影响仍然存在,这表明 Comamonas DA1877 产生了一种被线虫感知的信号。令人惊讶的是,这种发育效应与 TOR 和胰岛素信号无关。相反,Comamonas DA1877 通过核激素受体 NHR-23 影响蜕皮期间的循环基因表达。总之,我们的研究结果表明,不同的细菌通过不同的机制引发不同的反应,这对肥胖等疾病以及人类微生物组和肠道细胞之间的相互作用具有重要意义。